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Journal ArticleDOI

Tracing the cellular origin of cancer

Cédric Blanpain
- 01 Feb 2013 - 
- Vol. 15, Iss: 2, pp 126-134
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TLDR
This review explores how mouse genetic lineage-tracing experiments that allow the expression of oncogenes and/or the deletion of tumour suppressor genes in defined cell lineages have been instrumental in defining the cellular origin of different solid tumours in mouse models for various human cancers.
Abstract
Although many genes that lead to different types of cancer when mutated have been identified, the cells that initiate tumour formation following accumulation of these mutations have, until recently, remained elusive. This review explores how mouse genetic lineage-tracing experiments that allow the expression of oncogenes and/or the deletion of tumour suppressor genes in defined cell lineages have been instrumental in defining the cellular origin of different solid tumours in mouse models for various human cancers.

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Citations
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Demonstration of CRISPR/Cas9/sgRNA-mediated targeted gene modification in Arabidopsis, tobacco, sorghum and rice

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Dedifferentiation of committed epithelial cells into stem cells in vivo

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Cancer Stem Cells: Basic Concepts and Therapeutic Implications

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Defining the Hallmarks of Metastasis

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References
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Journal ArticleDOI

Temporally controlled ablation of PTEN in adult mouse prostate epithelium generates a model of invasive prostatic adenocarcinoma

TL;DR: The present mouse model, in which prostate carcinogenesis is initiated through Cre-ERT2-mediated somatic biallelic ablation of the tumor suppressor gene PTEN after puberty, closely mimics the course of human cancer formation.
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ROCK inhibitor Y-27632 suppresses dissociation-induced apoptosis of murine prostate stem/progenitor cells and increases their cloning efficiency.

TL;DR: The study implies that the numbers of prostate cells with stem/progenitor activity may be underestimated based on currently employed assays, supports that dissociation-induced apoptosis is a common feature of embryonic and somatic stem cells with an epithelial phenotype, and highlights the significance of environmental cues for the maintenance of stem cells.
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Suprabasal α6β4 integrin expression in epidermis results in enhanced tumourigenesis and disruption of TGFβ signalling

TL;DR: It is suggested that suprabasal α6β4 promotes tumourigenesis by preventing TGFβ from suppressing clonal expansion of initiated cells in the epidermal basal layer.
Journal ArticleDOI

Expression of Activated MEK1 in Differentiating Epidermal Cells Is Sufficient to Generate Hyperproliferative and Inflammatory Skin Lesions

TL;DR: The data suggest that activation of MEK1 downstream of beta1 integrins plays an important role in epidermal hyperproliferation and skin inflammation.
Journal ArticleDOI

Regenerated luminal epithelial cells are derived from preexisting luminal epithelial cells in adult mouse prostate.

TL;DR: Using prostate-specific antigen-CreER(T2)-based genetic lineage marking/tracing in mice, preexisting luminal epithelial cells were shown to be a source of regenerated luminalocyte cells in the adult prostate during androgen deprivation and replacement.
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Trending Questions (1)
Cancer is traced from when?

The paper does not explicitly mention when cancer is traced from. The paper discusses the cellular origin of cancer and how mouse genetic lineage-tracing experiments have helped in identifying the cells that initiate tumor formation.